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(Z)-2-(1-(3-methylphenyl)prop-1-en-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Base Information
  • Chemical Name:(Z)-2-(1-(3-methylphenyl)prop-1-en-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • CAS No.:1402235-26-0
  • Molecular Formula:C16H23BO2
  • Molecular Weight:258.168
  • Hs Code.:
(Z)-2-(1-(3-methylphenyl)prop-1-en-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Synonyms:(Z)-2-(1-(3-methylphenyl)prop-1-en-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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Chemical Property of (Z)-2-(1-(3-methylphenyl)prop-1-en-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Technology Process of (Z)-2-(1-(3-methylphenyl)prop-1-en-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

There total 3 articles about (Z)-2-(1-(3-methylphenyl)prop-1-en-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With C27H40Cl2FeN3P; sodium triethylborohydride; In pentane; at 20 ℃; for 8h; stereoselective reaction;
DOI:10.1021/acscatal.1c02432
Guidance literature:
With methanol; P(p-CH3OC6H4)3; copper(l) chloride; sodium t-butanolate; In diethyl ether; at 20 ℃; for 0.833333h; stereoselective reaction; Inert atmosphere;
DOI:10.1002/adsc.201100929
Guidance literature:
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; With 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; cobalt acetylacetonate; In tetrahydrofuran; at 20 ℃; for 0.25h; Inert atmosphere; Schlenk technique;
1-methyl-3-(prop-1-yn-1-yl)benzene; In tetrahydrofuran; at 20 ℃; for 16h; Overall yield = 83 percent; Overall yield = 85.48 mg; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.orglett.1c02854
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